A boy with dysmorphic features, intellectual disability, and biallelic homozygous deletion in NRXN1.

Research output: Contribution to journalArticle

Details

Authors
  • Peter Holmquist
Organisations
Research areas and keywords

Subject classification (UKÄ) – MANDATORY

  • Pediatrics
Original languageEnglish
Pages (from-to)75-78
JournalClinical Dysmorphology
Volume24
Issue number2
Publication statusPublished - 2015
Publication categoryResearch
Peer-reviewedYes